MORANDIPARK PANTHENOL ULTRA LIGHT SUNSCREEN - BRAND GENOME CO., Ltd.

Manufacturer
BRAND GENOME CO., Ltd.
Effective date
2026-06-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
monthly-update
Hydrated at
2026-07-17 21:35:38

Label at a glance#

ProductMORANDIPARK PANTHENOL ULTRA LIGHT SUNSCREEN
Active ingredientHOMOSALATE, OCTISALATE, OCTOCRYLENE, AVOBENZONE
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Directions
For sunscreen use
■ Apply liberally and evenly 15 minutes before sun exposure.
■ Reapply at least every 2 hours.
■ Sun Protection Measures.
Spending time in the sun increases your risk of skin cancer and early skin aging.
To decrease this risk, regularty use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
■ Limit time in the sun, especially from 10 a.m. -2 p.m.
■ Wear long-sleeved shirts, pants, hats, and sunglasses.
■ Children under 6 months of age: Ask a doctor
■ Use a water resistant sunscreen if swimming or sweating.

WARNINGS SECTION

Warnings
For external use only
Do not use ■
on damaged or broken skin.
When using this product ■ keep out of eyes. Rinse with water to remove.
Stop use and ask a doctor if ■ rash occurs.
Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.

INACTIVE INGREDIENT SECTION

WATER, BUTYLOCTYL SALICYLATE, DIPROPYLENE GLYCOL, PANTHENOL, DIETHYLHEXYL 2,6-NAPHTHALATE, C20-22 ALKYL PHOSPHATE, C20-22 ALCOHOLS, 1,2-HEXANEDIOL, SILICA, CAPRYLYL METHICONE, PENTYLENE GLYCOL, CETYL ALCOHOL, METHYL METHACRYLATE CROSSPOLYMER, GLYCERYL STEARATE, TROMETHAMINE, POLYACRYLATE CROSSPOLYMER-6, AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER, ETHYLHEXYLGLYCERIN, VP/EICOSENE COPOLYMER, TOCOPHEROL

INDICATIONS & USAGE SECTION

Uses
■ Helps prevent sunburn
■ If used as directed with other sun protection measures (see Directions),
decreases the risk of skin cancer and early skin aging caused by the sun.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.

OTC - PURPOSE SECTION

Sunscreen

RECENT MAJOR CHANGES SECTION

Typo on Directions:

" ~ other sun protection measures indluding:" > " ~ other sun protection measures including:"

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Secondary PackageSecondary Package

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87767-00187767-001-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 24 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12026-05-14daily-update2026-06-16 05:10:19

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MORANDIPARK PANTHENOL ULTRA LIGHT SUNSCREENHOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONEBRAND GENOME CO., Ltd.51c07375-e81d-8572-e063-6394a90ab5b02026-06-24WarningsExact identifier
ndc (package): 87767-001-01
ndc (product): 87767-001
ndc11 (package): 87767000101
spl id: 54fbed51-4f40-64be-e063-6294a90a1a0b
spl set id: 51c07375-e81d-8572-e063-6394a90ab5b0

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.